Sublingual Immunotherapy of Birch Pollen Associated Apple Allergy

Medical University of Vienna

Status and phase: Completed; Phase 2

Conditions: Birch Pollen Allergy; Birch Pollen Related Apple Allergy

Treatments: Drug: rMal d 1; Drug: rBet v 1; Other: placebo drops

Study type: Interventional

Funder types: Other

Identifiers

NCT01449786

TK01/2011

Details and patient eligibility

About

More than 70% of birch pollen allergic patients suffer from allergic reactions to certain foods, e.g. stone fruits, hazelnut and some vegetables. However, specific immunotherapy (SIT) with birch pollen extract is not effective for the treatment of associated food allergy in a substantial number of patients. Based on our previous clinical and immunological investigations of birch pollen related food allergy (BPRFA) the investigators hypothesize that for effective SIT of this abundant food allergy the disease-eliciting food allergens should be employed. To prove this concept, the investigators aim to sublingually administer the major apple allergen, Mal d 1, to birch pollen-allergic patients with concomitant apple allergy and evaluate clinical and immunological effects of this treatment. The investigators choose Mal d 1 as model food allergen because (i) its cross-reactivity with Bet v 1 has been well characterized,(ii) apple is the most frequent trigger for BPRFA and (iii) recombinant(r)Mal d 1 was well tolerated after sublingual administration to 20 birch pollen-allergic patients in a previous study. Sublingual administration of a defined concentration of GMP-rMal d 1 will be compared with equal doses of GMP-rBet v 1 as a positive control and placebo-treatment. Clinical parameters will include skin prick tests (SPT) and objective and subjective assessment of apple and birch pollen-induced allergic symptoms. Immunological parameters will comprise the analysis of antibody and T cell responses to Mal d 1 and Bet v 1 as well as the evaluation of basophil activation.

The proposed pilot study will be a first investigation of the concept to specifically treat BPRFA with the involved food allergens and thus, represents an important step in the development of an efficient and safe therapy in the future.

Enrollment: 60 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• otherwise healthy persons between 18 und 50 years of age;
• positive history of rhinoconjunctivitis to birch pollen
• oral allergy syndrome(OAS) to apple
• positive skin prick test (SPT) reaction to birch pollen and apple
• specific IgE for Bet v 1 and Mal d 1

Exclusion criteria

• Exclusion criteria
• Persons who due to their physical or mental state are not able to provide informed consent.
• Persons with underlying illnesses such as severe cardiopulmonary, malignant and/or autoimmune diseases
• Persons suffering from Hyper-IgE syndrome
• Persons receiving SIT during the past 5 years
• persons suffering from severe allergic reactions to apple such as generalized urticaria, asthma and/or anaphylaxis
• persons suffering from severe bronchial asthma to birch pollen
• persons suffering from pathological alterations of the lips and oral mucosa
• persons who are prescribed a treatment with immune-suppressive drugs, anti-histamines, leukotriene-antagonists or psychotropic drugs with anti-histaminic effects
• persons using ß-blockers
• Pregnant woman

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

60 participants in 3 patient groups, including a placebo group

treatment with rMal d 1

Experimental group

Description:

these apple and birch pollen allergic patients are treated with daily sublingual application of 25µg recombinant Major apple allergen, Mal d 1 during 4 months

Treatment:

Drug: rMal d 1

treatment with rBet v 1

Active Comparator group

Description:

These apple and birch pollen allergic patients are treated with daily sublingual application of 25µg recombinant Major birch pollen allergen,Bet v 1 during 4 months

Treatment:

Drug: rBet v 1

treatment with placebo drops

Placebo Comparator group

Description:

These apple and birch pollen allergic patients are treated daily with placebo applied sublingually during 4 months

Treatment:

Other: placebo drops